Pharmacy Jobs

Roles & Responsibilities • Manage clinical trial databases ensuring accurate and high-quality data flow • Perform data review, cleaning, and validation activities • Design, develop, and review eCase Report Forms (eCRFs) • Ensure compliance with ICH-GCP, ICH, EU, and FDA regulatory guidelines • Support study start-up, maintenance, and close-out activities • Collaborate with cross-functional teams to maintain data integrity • Contribute to audit readiness and regulatory inspection support • Maintain proper documentation throughout the clinical trial lifecycle Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related scientific discipline Experience • Minimum 1 year of experience as a Clinical Data Manager or Data Management Associate • Equivalent combination of education, training, and experience may be considered Skills • Strong knowledge of clinical data management processes • Understanding of end-to-end clinical trial lifecycle • Hands-on experience with clinical trial databases and CDMS tools • Sound knowledge of ICH-GCP and global regulatory requirements • Excellent documentation, communication, and coordination skills • Fluent in English (written and spoken) • Ability to work collaboratively in cross-functional teams About the Organisation Excelya is a fast-growing, global Contract Research Organization (CRO) known for its people-centric culture and strong presence in Europe and India. The company supports global clinical trials in regulatory-compliant environments, offering professionals long-term career growth, exposure to international studies, hybrid work flexibility, and continuous learning opportunities within a collaborative and inclusive workplace.

Roles & Responsibilities • Maintain thorough knowledge of Pharmacovigilance and Medical Information procedures, legal requirements, and quality documents • Handle adverse event reports and PV data in line with local regulations and company standards • Provide accurate and timely safety information to Health Authorities and relevant stakeholders • Support the Country Safety Head in local safety surveillance, risk management, and safety issue handling • Manage product alerts and market research programs with appropriate regulatory communication • Respond to Medical Information inquiries from healthcare professionals, patients, and customers with high-quality, compliant responses • Collaborate effectively with internal teams and external third parties within PV and Medical Information functions • Actively contribute to North Europe Cluster PV & Medical Information projects and daily operations Qualification • University degree in Pharmacy, Medicine, or an equivalent scientific discipline Experience • Prior experience in the pharmaceutical industry or equivalent • Experience in Pharmacovigilance, Drug Safety, or Medical Information preferred Skills • Strong knowledge of pharmacovigilance regulations and medical information processes • Excellent planning, organization, and attention-to-detail skills • High accuracy and compliance-oriented work approach • Strong interpersonal and communication skills for interaction with HCPs, patients, and internal teams • Proficiency in MS Office and relevant safety/MI systems • Ability to work collaboratively in cross-functional and multicultural teams • Fluency in English and Norwegian (written and spoken) About the Organisation Sanofi is an R&D-driven, AI-powered global biopharmaceutical company dedicated to improving lives through innovative medicines and vaccines. With deep expertise in immunology and a strong pipeline across diabetes, transplant, cardiovascular, and specialty care, Sanofi delivers treatments to more than 100 million people annually, combining global scale with local impact and a strong culture of collaboration, inclusion, and scientific excellence.

Roles & Responsibilities • Develop, program, validate, and maintain clinical trial databases in compliance with company SOPs and regulatory standards • Design and maintain CDASH-compliant Case Report Forms (CRFs) and support the standard CRF library • Perform Medidata RAVE study build activities including database setup, edit checks, and custom functions • Develop and implement custom functions using C# programming within Medidata RAVE • Act as the primary technical point of contact for Data Management teams on assigned clinical studies • Ensure high-quality database design, validation documentation, and audit readiness • Provide technical support throughout the clinical trial lifecycle from study startup to database lock • Support global clinical trials across multiple therapeutic areas Qualification • Bachelor’s or Advanced degree in Life Sciences, Computer Science, or equivalent Experience • Minimum 3+ years of experience in Clinical Database Programming • Hands-on experience in Medidata RAVE study build and maintenance • Experience working in CRO, pharma, or biotech clinical research environments Skills • Strong expertise in Medidata RAVE (study build, edit checks, custom functions) • Proficiency in Custom Functions and C# programming • Knowledge of CDASH standards and CRF design principles • Familiarity with Veeva EDC is an added advantage • Understanding of clinical data management and regulatory requirements • Excellent documentation and validation skills • Strong attention to detail and quality mindset • Effective communication and cross-functional collaboration skills About the Organisation Medpace is a globally recognized Clinical Research Organization (CRO) with more than three decades of experience supporting Phase I–IV clinical trials across multiple therapeutic areas. Known for its scientific-driven approach and strong in-house expertise, Medpace offers a stable, growth-oriented environment where clinical research professionals can build long-term careers while contributing to global drug development programs.

Roles & Responsibilities • Analyze organizational processes, business models, and system integrations with technology • Act as Subject Matter Expert (SME) in Drug Safety and Pharmacovigilance for Veeva Vault Safety • Lead requirement-gathering workshops and define system requirements for Veeva Vault implementation • Assess current-state processes and define future-state business solutions aligned with regulatory needs • Design and configure Veeva Vault to meet FDA, EMA, and ICH regulatory requirements • Document business and system requirements including URS, FS, and user stories • Develop test scripts and support system validation and UAT activities • Serve as the primary liaison between customers, stakeholders, and delivery teams • Collaborate with Product Owners to manage backlogs, prioritize user stories, and support agile delivery • Participate in RFPs and support business development initiatives • Ensure compliance with global Drug Safety and Pharmacovigilance regulations • Provide post-implementation support and optimization for Veeva Vault Safety solutions • Lead change management activities to support client transition to Veeva Vault • Define deployment strategies and post–go-live support plans • Mentor and guide cross-functional teams to ensure successful project delivery Qualification • 15 years of full-time education (Bachelor’s degree or equivalent) Experience • Minimum 5 years of experience in Business Requirements Analysis • Hands-on experience as a Life Sciences / Pharmacovigilance Business Analyst • Experience working on Drug Safety and Pharmacovigilance systems preferred Skills • Strong expertise in Business Requirements Analysis • In-depth knowledge of Pharmacovigilance & Drug Safety Surveillance • Hands-on experience with Veeva Vault Safety • Familiarity with PV systems such as Argus, ArisGlobal • Knowledge of GxP, ICH, FDA, EMA, and global safety regulations (ICH E2E) • Understanding of medical terminology and safety dictionaries (MedDRA, WHO Drug) • Experience with Agile delivery models and backlog management • Proficiency in tools such as JIRA, Confluence, HP-ALM, Q-Test • Working knowledge of SQL, Oracle, XML, Medidata, TMF, eCRF • Strong documentation, communication, and stakeholder management skills • Leadership, mentoring, and cross-functional collaboration abilities • Strong analytical, critical thinking, and problem-solving skills About the Organisation The organization operates at the intersection of life sciences and digital transformation, delivering technology-enabled solutions for Pharmacovigilance, Drug Safety, and regulatory compliance. With a strong focus on Veeva Vault implementations and global regulatory standards, it supports pharmaceutical and life sciences clients in optimizing safety operations, ensuring compliance, and driving efficient, high-quality system delivery across global programs.

Roles & Responsibilities • Perform routine analytical testing of in-process and isolated samples • Analyze early intermediates and APIs using chromatographic and wet analytical techniques • Execute method qualification and support instrument calibration activities • Maintain accurate and compliant documentation using Electronic Lab Notebooks (ELN) • Ensure adherence to GxP guidelines and quality standards • Handle general laboratory responsibilities and support ongoing Analytical R&D activities • Contribute to API development and chemical research programs Qualification • M.Pharm (Pharmaceutical Analysis / Analytical Chemistry preferred) Experience • Relevant experience in Analytical R&D within pharmaceutical or CRO/CRDMO environments preferred Skills • Strong theoretical and practical knowledge of analytical chemistry • Hands-on experience with chromatographic techniques • Understanding of method qualification and instrument calibration • Knowledge of GxP documentation and compliance standards • Proficiency in MS Office tools (Word, Excel, PowerPoint) • Strong communication, documentation, and teamwork skills • High attention to detail with a proactive and ethical work approach • Willingness to work in shifts, if required About the Organisation Syngene International Ltd. is a leading global Contract Research, Development, and Manufacturing Organization (CRDMO) supporting pharmaceutical and biotechnology companies worldwide. Known for its strong scientific capabilities and innovation-driven culture, Syngene offers professionals exposure to cutting-edge API development, analytical research, and global drug discovery programs.

Roles & Responsibilities:• Convert patient health information into accurate alphanumeric medical codes• Review medical reports including diagnosis, procedures, and prescriptions• Assign ICD-10, CPT, and HCPCS codes as per medical documentation• Ensure accuracy and compliance with medical coding guidelines• Support medical claims processing and healthcare documentation• Maintain confidentiality of patient and medical recordsQualifications & Experience:• UG / PG graduates from Life Science, Paramedical, or Medical background• Eligible streams include BDS, BPT, Nursing (GNM/DGNM), Pharmacy, Physiotherapy, Biotechnology, Microbiology, Biochemistry, Biomedical, Bioinformatics, Zoology, Botany, Biology, Medical Lab Technology, Radiology, Dialysis, Cardiac Care, OT & Anaesthesia Technology, Physician Assistant, and related courses• Freshers and recent pass-outs (2016–2025) are eligibleSkills Required:• Basic knowledge of Anatomy and Physiology• Good communication and interpersonal skills• Basic computer and documentation skills• Willingness to learn medical coding standards• Attention to detail and accuracyBenefits & Perks:• System-based desk job• 5-day work week (Saturday & Sunday off)• Day shift only• Food and cab facility provided• Performance-based incentives• Salary increment after 6 months for experienced candidates• PF and medical insurance benefits• Gratuity after 5 years• Referral bonus available• Overseas job opportunitiesJob Locations:• Chennai, Coimbatore, Vellore, Trichy, Salem, Erode, Thanjavur• Tirunelveli, Nagercoil, Villupuram, Karur, Theni• Tirupati, Andhra Pradesh, Telangana, Kerala, Tamil NaduAbout the Company:• Achievers Spot is an ISO 9001:2015 certified medical coding training and placement organization based in Chennai.• The company provides classroom and certification-based training in ICD-10, CPT, HCPCS, Anatomy, Physiology, and Medical Coding.• Achievers Spot has successfully placed candidates in leading healthcare BPOs and MNCs across India, offering strong career growth in the healthcare IT sector.

Roles & Responsibilities:• Look after physiotherapy machines and equipment, ensuring proper functioning and maintenance• Assist patients during therapy sessions and monitor their progress• Provide safe and effective physiotherapy treatments tailored to patient needs• Educate patients on exercises and rehabilitation techniques• Maintain accurate patient records and document therapy sessions• Coordinate with other healthcare professionals as requiredQualifications:• Bachelor’s degree in Physical Education (B.P.Ed), Pharmacy (B.Pharm), BAMS, or any relevant field• Postgraduate degree (MS / M.Sc) in any specialization preferredExperience:• 1 – 3 years of experience in physiotherapy, patient care, or healthcare support• Experience handling physiotherapy machines is preferredSkills Required:• Knowledge of physiotherapy techniques and rehabilitation exercises• Ability to operate physiotherapy equipment safely• Strong patient-handling and interpersonal skills• Professional, ethical, and patient-focused approachAbout the Company:• The company operates in the healthcare sector, providing patient care services and supporting rehabilitation and physiotherapy treatments.

Roles & Responsibilities • Process, triage, and track ICSRs as per SOPs and safety plans • Enter safety data into databases and perform MedDRA coding • Review cases for completeness, accuracy, and regulatory reportability • Prepare case narratives and manage follow-up queries • Support expedited safety reporting and literature case processing • Identify and manage duplicate cases • Support xEVMPD, SPOR/IDMP, and drug dictionary activities • Ensure TMF and PV system documentation compliance • Participate in audits and maintain regulatory compliance Qualification • B.Pharm / M.Pharm / PharmD / BDS Experience • Minimum 2 years in Pharmacovigilance or Safety Case Processing Skills • Strong PV and safety reporting knowledge • Experience with safety databases and medical terminology • Knowledge of ICH-GCP, GVP, and global PV regulations • Good communication, documentation, and time-management skills About the Organisation Syneos Health® is a global biopharmaceutical solutions organization supporting clinical development, medical affairs, and commercialization. With operations across 110 countries, Syneos Health is recognized for its patient-centric approach, regulatory expertise, and strong career development culture.

Roles & Responsibilities • Monitor raw material dispensing activities in compliance with SOPs and cGMP requirements • Perform daily IPQA activities as per defined frequencies and ensure timely closure of observations • Carry out validation sampling as per approved validation protocols • Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) for accuracy and regulatory compliance • Execute ERP-related IPQA transactions, preferably using SAP or equivalent systems • Verify Batch Summary Records (BSR) and perform shipper inspections as per SOPs • Manage issuance, review, reconciliation, and control of QA formats across departments • Conduct regular IPQA rounds, communicate observations to HODs, and support corrective actions • Ensure cleaning, sanitation, and hygiene practices to maintain continuous GMP compliance • Perform sampling of In-Process materials, Semi-Finished Goods (SFG), and Finished Goods (FG) as per procedures Qualification • B.Pharm / M.Pharm / M.Sc in a relevant discipline Experience • 2–5 years of experience in IPQA or Quality Assurance within the pharmaceutical industry Skills • Strong knowledge of IPQA processes, cGMP, and regulatory guidelines • Excellent documentation, review, and compliance skills • Hands-on experience with ERP systems, preferably SAP • Good communication and cross-functional coordination abilities • Ability to conduct inspections, identify deviations, and support corrective and preventive actions About the Organisation Shalina Healthcare is a reputed pharmaceutical company with a strong global presence, committed to delivering high-quality, affordable healthcare products. The organization operates in regulated manufacturing environments and emphasizes strict GMP compliance, continuous improvement, and professional growth, offering employees hands-on exposure to quality systems and international regulatory standards.

Roles & Responsibilities • Act as the primary point of contact for internal teams, sponsors, and external vendors • Manage clinical data timelines, deliverables, and project milestones • Ensure data integrity and quality across EDC and ePRO systems • Perform clinical data review, ePRO review, query generation, resolution, and reconciliation • Support database transfers, data exports, and migrations • Prepare and maintain Data Management Plans (DMP), CRF specifications, and training documents • Participate in Site Initiation Visits (SIVs) and conduct site trainings • Support User Acceptance Testing (UAT) and product launches • Ensure compliance with GCP, ICH, HIPAA, GDPR, FDA 21 CFR Part 11, and Annex 11 • Assist in internal and external audits and respond to compliance findings • Explore and support innovative approaches for remote and decentralized clinical trials Qualification • Undergraduate degree from an accredited university • Preferred background in Life Sciences, Pharmacy, Biotechnology, or Computer Science Experience • 0–10 years of experience in Clinical Data Management, Clinical Research, or CRO environment • Exposure to clinical trials, observational studies, or registries preferred Skills • Hands-on knowledge of EDC, ePRO, and EHR systems • Familiarity with data standards such as CDISC, SDTM, FHIR, and OMOP • Knowledge of MedDRA and WHO Drug coding dictionaries • Strong understanding of clinical trial data workflows • Good project management and organizational skills • Strong communication and problem-solving abilities • Ability to work independently in a remote environment Preferred Skills • Experience in rare diseases, gene therapy, or long-term follow-up studies • Experience working with central labs or specialty vendors • Exposure to digital health tools or mobile applications About the Organisation A leading organization in clinical research and healthcare data solutions, focused on delivering high-quality, compliant, and innovative clinical data management services to support global clinical trials.

Roles & Responsibilities • Dispense medicines accurately as per prescriptions and government health guidelines • Maintain proper storage conditions for drugs, vaccines, and medical supplies • Manage pharmacy inventory, stock registers, and medicine distribution records • Ensure availability of essential medicines and monitor expiry dates • Follow standard operating procedures and statutory pharmacy regulations • Assist medical officers and healthcare staff in medication-related matters • Ensure cleanliness, safety, and organization of the pharmacy area Qualification • Bachelor of Pharmacy (B. Pharm) from a recognized university • Registration with the State Pharmacy Council is mandatory Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per organisation norms Application Fee • All Other Candidates: Rs. 100/- • SC / ST / OBC Candidates: Rs. 50/- Important Date • Application Deadline: 09-02-2026Skills • Sound knowledge of pharmaceutical drugs and dispensing practices • Good inventory and stock management skills • Attention to detail and accuracy in medication handling • Basic computer knowledge for data entry and record maintenance • Good communication and coordination skills About the Organisation District Health & Family Welfare Samiti (DHFWS) operates under the National Health Mission and is responsible for implementing public health programs, strengthening healthcare delivery systems, and ensuring accessible medical services at the district level.Official NotificationClick Here

Roles & Responsibilities • Assist in planning and execution of sponsored research projects • Conduct laboratory experiments, data collection, and scientific analysis • Maintain accurate documentation of research activities and results • Support preparation of research reports, manuscripts, and presentations • Ensure compliance with institutional guidelines and research protocols • Coordinate with faculty members, project investigators, and research teams • Maintain laboratory equipment, instruments, and research materials • Contribute to innovation, problem-solving, and continuous improvement in research outcomes Qualification • M. Pharm or M.Sc in a relevant discipline Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per organization norms Important Date • Application Deadline: 24-01-2026Skills • Strong knowledge of pharmaceutical sciences / life sciences research concepts • Hands-on laboratory skills and experimental techniques • Data analysis and interpretation skills • Research documentation and scientific writing skills • Familiarity with basic statistical tools and software • Ability to follow SOPs, safety protocols, and ethical research practices About the Organization BITS Pilani is one of India’s premier institutes of higher education and research, renowned for excellence in science, engineering, technology, and innovation. The institute actively promotes cutting-edge research and interdisciplinary collaboration to address real-world challenges.Official NotificationClick Here

Roles & Responsibilities • Dispense medicines accurately as per prescriptions and ECHS guidelines • Maintain proper storage, labeling, and inventory control of pharmaceutical supplies • Ensure compliance with government healthcare and pharmacy regulations • Monitor drug stock levels, expiry dates, and maintain pharmacy records • Assist doctors and healthcare staff in providing effective patient care • Ensure safe handling, dispensing, and counseling of medicines • Support smooth functioning of pharmacy services under ECHS Qualification • B. Pharm or D. Pharm Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per organization norms Important Date • Application Deadline: 28-01-2026 Walk-in Address OIC, Stn HQ (ECHS CELL), CAD Pulgaon, Teh - Deoli, Distt - Wardha, Maharashtra - 442303 About the Organization The Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India initiative that provides comprehensive healthcare services to ex-servicemen and their dependents through a network of polyclinics across the country.Official NotificationClick Here

Roles & Responsibilities • Dispense medicines accurately as per prescribed treatment guidelines • Maintain proper storage, labeling, and inventory management of medicines • Ensure compliance with AYUSH and government healthcare regulations • Monitor drug stock levels, expiry dates, and maintain pharmacy records • Assist doctors and healthcare staff in pharmaceutical care services • Ensure safe handling and dispensing of medicines • Support National AYUSH Mission healthcare initiatives at the hospital level Qualification • Bachelor of Pharmacy (B. Pharm) Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per government norms Important Date • Application Deadline 30-01-2026 Walk-in  Address District Homoeo Hospital Building, Kalpathy, Palakkad About the Organization National AYUSH Mission (NAM), Kerala is a government initiative aimed at strengthening AYUSH healthcare services across the state. The mission focuses on improving access to quality traditional and alternative healthcare systems through well-equipped hospitals, trained professionals, and community-based health programs.Official Notification and Application FormClick Here

Roles & Responsibilities • Dispense medicines accurately as per prescriptions and treatment protocols • Maintain proper storage, labeling, and inventory control of medicines • Ensure compliance with government healthcare and pharmacy regulations • Maintain stock registers, issue records, and drug expiry monitoring • Assist medical officers in pharmaceutical care and patient counseling • Ensure safe handling of drugs and medical supplies • Support public health programs implemented by the District Health Society Qualification • D. Pharm Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per government norms Important Date • Application Deadline: 06-02-2026 Address District Health Society and District Health Officer, District Health Office, Near LIC Building, Thanjavur – 613 001 About the Organization District Health Society (DHS), Thanjavur operates under the public health system of Tamil Nadu and is responsible for implementing national and state health programs. The organization plays a vital role in strengthening healthcare delivery, ensuring availability of essential medicines, and promoting community health services at the district level.Official NotificationClick Here

Roles & Responsibilities • Deliver undergraduate and postgraduate teaching in assigned pharmacy subjects • Prepare lesson plans, lecture materials, practical manuals, and assessments • Evaluate student performance through examinations, assignments, and projects • Guide students in academic, research, and career development activities • Engage in research activities and publish in reputed journals • Participate in curriculum development and academic planning as per PCI/University norms • Support accreditation, inspections, and quality assurance activities • Contribute to institutional committees, seminars, workshops, and conferences • Mentor students and promote a positive learning environment Qualification • M.Pharm or PharmD Experience • Freshers or experienced candidates as per PCI norms Skills • Strong subject knowledge in pharmacy discipline • Effective teaching, communication, and presentation skills • Interest in research and academic development • Ability to mentor and guide students • Familiarity with academic regulations and accreditation requirements About the Institute St. Peter's Institute of Pharmaceutical Sciences (Autonomous) is a reputed academic institution committed to excellence in pharmacy education, research, and professional development. The institute focuses on nurturing skilled pharmacy professionals through quality teaching, innovation-driven research, and industry-aligned academic practices to shape future leaders in the pharmaceutical and healthcare sectors.📩 Send your CV to: principal@stpeters.co.in

Roles & Responsibilities • Dispense medicines accurately as per prescriptions and treatment protocols • Ensure proper storage, labeling, and handling of medicines and medical supplies • Maintain pharmacy stock records, inventory registers, and consumption data • Monitor expiry dates and ensure timely replenishment of medicines • Counsel patients on correct medication usage, dosage, and precautions • Ensure compliance with government healthcare guidelines and standard operating procedures • Coordinate with doctors, nurses, and healthcare staff for effective patient care • Maintain cleanliness, safety, and regulatory compliance within the pharmacy Qualification • B.Pharm or D.Pharm Age Limit • Minimum Age: 18 Years • Maximum Age: 45 Years • Age relaxation applicable as per Government / Organisation norms Important Date• Application Deadline: 06-02-2026Skills • Knowledge of pharmaceutical drugs and formulations • Good communication and patient counseling skills • Basic understanding of inventory and stock management • Ability to work in a public healthcare setup • Attention to detail and compliance with healthcare standards About the Company District Health Society (DHS), Thanjavur operates under the National Health Mission (NHM) and is responsible for implementing public health programs at the district level. DHS focuses on improving healthcare delivery, ensuring availability of essential medicines, and strengthening public health infrastructure to provide accessible and quality healthcare services to the community.Official Notification Click Here

Key Responsibilities • Process and triage Individual Case Safety Reports (ICSRs) as per SOPs and safety plans • Perform case data entry, MedDRA coding, and narrative writing • Conduct literature screening and safety reviews • Identify, manage, and reconcile duplicate ICSRs • Perform quality review of safety cases • Support xEVMPD submissions and SPOR/IDMP activities • Maintain safety trackers and ensure regulatory compliance (ICH GCP, GVP) • Submit documents to TMF and PSMF • Participate in audits and regulatory inspections • Collaborate with global cross-functional PV teams Education: • B.Pharm / M.Pharm / Pharm.D / BDSExperience: • Specialist I: 2+ years • Specialist II: 3.5+ yearsTechnical Skills: • Strong knowledge of ICH, GVP, and global PV regulations • Hands-on experience with safety databases • Understanding of Clinical Trial phases II–IV and post-marketing safety • Proficiency in MS Word, Excel, PowerPoint, OutlookSoft Skills: • Excellent communication and documentation skills • Strong attention to detail and organizational ability Why Join Syneos Health? • Work on global studies involving 675,000+ clinical trial patients • Exposure to global audits, inspections, and regulatory submissions • Strong internal mobility and career development programs • Inclusive Total Self culture promoting diversity and well-being • Competitive compensation and rewards

Key Responsibilities • Process and triage Individual Case Safety Reports (ICSRs) as per SOPs and safety plans • Perform case data entry, MedDRA coding, and narrative writing • Conduct literature screening and safety reviews • Identify, manage, and reconcile duplicate ICSRs • Perform quality review of safety cases • Support xEVMPD submissions and SPOR/IDMP activities • Maintain safety trackers and ensure regulatory compliance (ICH GCP, GVP) • Submit documents to TMF and PSMF • Participate in audits and regulatory inspections • Collaborate with global cross-functional PV teamsEducation: • B.Pharm / M.Pharm / Pharm.D / BDS Experience• Specialist I: 2+ yearsTechnical Skills: • Strong knowledge of ICH, GVP, and global PV regulations • Hands-on experience with safety databases • Understanding of Clinical Trial phases II–IV and post-marketing safety • Proficiency in MS Word, Excel, PowerPoint, Outlook Soft Skills: • Excellent communication and documentation skills• Strong attention to detail and organizational abilityWhy Join Syneos Health? • Work on global studies involving 675,000+ clinical trial patients • Exposure to global audits, inspections, and regulatory submissions • Strong internal mobility and career development programs • Inclusive Total Self culture promoting diversity and well-being • Competitive compensation and rewards